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4-Chloro-5-(3-dimethylaminomethyl-pyrrolidin-1-yl)-2-nitroaniline → 4-Chloro-5-(3-dimethylaminomethyl-pyrrolidin-1-yl)-benzene-1,2-diamine

HRID 1258638
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반응식

HRID 1258638 반응식
[Cl:1][C:2]1[C:8]([N:9]2[CH2:13][CH2:12][CH:11]([CH2:14][N:15]([CH3:17])[CH3:16])[CH2:10]2)=[CH:7][C:5]([NH2:6])=[C:4]([N+:18]([O-])=O)[CH:3]=1>[Ni].CCOC(C)=O>[Cl:1][C:2]1[CH:3]=[C:4]([NH2:18])[C:5]([NH2:6])=[CH:7][C:8]=1[N:9]1[CH2:13][CH2:12][CH:11]([CH2:14][N:15]([CH3:16])[CH3:17])[CH2:10]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 679579424-Chloro-5-(3-dimethylaminomethyl-pyrrolidin-1-yl)-2-nitroaniline

생성물 1

HCID 679579304-Chloro-5-(3-dimethylaminomethyl-pyrrolidin-1-yl)-benzene-1,2-diamine

시약·촉매·용매 2

HCID 935Nickel촉매HCID 8857Ethyl Acetate용매

실험 절차

A mixture of 4-chloro-5-(3-dimethylaminomethyl-pyrrolidin-1-yl)-2-nitroaniline (630 mg, 2.1 mmol), EtOAc (20 mL) and Ra—Ni (150 mg) was stirred for 2 days at rt under a hydrogen atmosphere (3.0 bar). The catalyst was removed by filtration and the filtrate was concentrated. The crude was purified by chromatography to give the sub-title compound.

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후처리

  1. customThe catalyst was removed by filtration
  2. concentrationthe filtrate was concentrated
  3. customThe crude was purified by chromatography

출처 및 근거

ORD 기록
ord-1adaa7f3ad76482bb3cf3a0f30e9933e
출처 데이터셋
uspto-grants-2013_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08466186B2

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